Regional Medical Advisor

Abbott; Delhi; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Abbott in India seeks an experienced Medical Affairs professional who executes clinical trials, manages data collection, and ensures compliant study conduct under supervision.

You will guide protocol implementation, coordinate investigators, manage reporting to regulators, and support safety monitoring across Phases III and IV.

Responsibilities

• Oversee direction, planning, execution of clinical trials/research and data collection.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Direct human clinical trials, Phases III & IV for company products under development.
• Participates in adverse event reporting and safety monitoring.
• Coordinates and provides reporting information for regulatory submissions.
• Monitors adherence to protocols and determines study completion.
• Coordinates and oversees investigator initiations and group studies.
• May participate in adverse event reporting and safety monitoring.
• May act as a consultant/liaison with other corporations under licensing agreements.

Job description

Main Purpose of the Role

Summarize the main purpose of the role

Experienced professional individual contributor that works under limited supervision.

Applies subject matter knowledge in the area of Medical Affairs.

Requires capacity to apply skills/knowledge within the context of specific needs or requirements.

Main Responsibilities

• List the main responsibilities this role regularly performs.
  • As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
  • Contributes to implementation of clinical protocols, and facilitates completion of final reports.
  • Recruits clinical investigators and negotiates study design and costs.
  • Responsible for directing human clinical trials, phases III & IV for company products under development.
  • Participates in adverse event reporting and safety responsibilities monitoring.
  • Coordinates and provides reporting information for reports submitted to the regulatory agencies.
  • Monitors adherence to protocols and determines study completion.
  • Coordinates and oversees investigator initiations and group studies.
  • May participate in adverse event reporting and safety responsibilities monitoring.
  • May act as consultant/liaison with other corporations when working under licensing agreements.